Canonical Allele Identifier: CA2244628659

Gene: ENO3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4955446_4955447delinsAC , CM000679.2:g.4955446_4955447delinsAC	GRCh38
NC_000017.10:g.4858741_4858742delinsAC , CM000679.1:g.4858741_4858742delinsAC	GRCh37
NC_000017.9:g.4799487_4799488delinsAC	NCBI36
NG_012063.2:g.14356_14357delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519602.6:c.707_708delinsAC MANE Select	ENSP00000430055.2:p.Tyr236=
ENST00000323997.10:c.707_708delinsAC	ENSP00000324105.6:p.Tyr236=
ENST00000518175.1:c.707_708delinsAC	ENSP00000431087.1:p.Tyr236=
ENST00000519584.5:c.578_579delinsAC	ENSP00000430636.1:p.Tyr193=
ENST00000519602.5:c.707_708delinsAC	ENSP00000430055.1:p.Tyr236=
ENST00000521659.5:c.*653_*654delinsAC	ENSP00000430554.1:n.*653_*654delinsAC
NM_001193503.1:c.578_579delinsAC	NP_001180432.1:p.Tyr193=
NM_001976.4:c.707_708delinsAC	NP_001967.3:p.Tyr236=
NM_053013.3:c.707_708delinsAC	NP_443739.3:p.Tyr236=
XM_005256521.2:c.734_735delinsAC	XP_005256578.1:p.Tyr245=
XM_011523729.1:c.707_708delinsAC	XP_011522031.1:p.Tyr236=
XM_017024346.2:c.707_708delinsAC	XP_016879835.1:p.Tyr236=
NM_001193503.2:c.578_579delinsAC	NP_001180432.1:p.Tyr193=
NM_001374523.1:c.707_708delinsAC	NP_001361452.1:p.Tyr236=
NM_001374524.1:c.734_735delinsAC	NP_001361453.1:p.Tyr245=
NM_001976.5:c.707_708delinsAC	NP_001967.3:p.Tyr236=
NM_053013.4:c.707_708delinsAC MANE Select	NP_443739.3:p.Tyr236=